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23805-51-8

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23805-51-8 Usage

Type of compound

Chemical compound

Uses

Commonly used as an antiseptic and disinfectant

Effectiveness

Effective against a wide range of bacteria and viruses

Applications

Household cleaning products, medical and veterinary settings

Mechanism of action

Disrupts the cell membranes of microorganisms

Additional uses

Ingredient in personal care products such as soaps and lotions

Safety precautions

Should be used with caution and according to product label instructions to avoid excessive exposure and potential harm.

Check Digit Verification of cas no

The CAS Registry Mumber 23805-51-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,0 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23805-51:
(7*2)+(6*3)+(5*8)+(4*0)+(3*5)+(2*5)+(1*1)=98
98 % 10 = 8
So 23805-51-8 is a valid CAS Registry Number.

23805-51-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-chlorophenyl)methyl]-4-methylphenol

1.2 Other means of identification

Product number -
Other names 2-(4-Chlor-benzyl)-4-methyl-phenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23805-51-8 SDS

23805-51-8Relevant articles and documents

2-(Dihalobenzyl)-6-nitro-4-t-butylphenol and preparation thereof

-

, (2008/06/13)

The specification describes novel 2-(4'-halobenzyl) phenols of the formula: SPC1 In which R1, R2 and R3, which may be the same or different,re hydrogen or a lower alkyl group, provided that only one of R1 , R2 and R3 is hydrogen, or any two or R1, R2 and R3 form, together with the carbon atom to which they are attached, a cycloalkyl ring, particularly cyclohexyl, and the third substituent is hydrogen; R4 is hydrogen, halogen, a nitro group or a benzyl group, the latter, if desired, being substituted in the same manner as the benzyl group shown in the ortho position of the phenolic nucleus; R5 is hydrogen or a hydroxyl group; X is halogen, particularly chlorine or bromine, and Y is hydrogen or halogen, particularly chlorine or bromine, and a process for their preparation. These compounds have useful bacteriostatic activity.

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